International Journal of Endocrinology

International Journal of Endocrinology / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 846742 |

Yu Fu, Jing Luo, Zhenquan Jia, Wei Zhen, Kequan Zhou, Elizabeth Gilbert, Dongmin Liu, "Baicalein Protects against Type 2 Diabetes via Promoting Islet β-Cell Function in Obese Diabetic Mice", International Journal of Endocrinology, vol. 2014, Article ID 846742, 13 pages, 2014.

Baicalein Protects against Type 2 Diabetes via Promoting Islet β-Cell Function in Obese Diabetic Mice

Academic Editor: Hyun C. Lee
Received07 Apr 2014
Revised07 Jul 2014
Accepted14 Jul 2014
Published23 Jul 2014


In both type 1 (T1D) and type 2 diabetes (T2D), the deterioration of glycemic control over time is primarily caused by an inadequate mass and progressive dysfunction of β-cell, leading to the impaired insulin secretion. Here, we show that dietary supplementation of baicalein, a flavone isolated from the roots of Chinese herb Scutellaria baicalensis, improved glucose tolerance and enhanced glucose-stimulated insulin secretion (GSIS) in high-fat diet (HFD-) induced middle-aged obese mice. Baicalein had no effect on food intake, body weight gain, circulating lipid profile, and insulin sensitivity in obese mice. Using another mouse model of type 2 diabetes generated by high-fat diet (HFD) feeding and low doses of streptozotocin injection, we found that baicalein treatment significantly improved hyperglycemia, glucose tolerance, and blood insulin levels in these middle-aged obese diabetic mice, which are associated with the improved islet β-cell survival and mass. In the in vitro studies, baicalein significantly augmented GSIS and promoted viability of insulin-secreting cells and human islets cultured either in the basal medium or under chronic hyperlipidemic condition. These results demonstrate that baicalein may be a naturally occurring antidiabetic agent by directly modulating pancreatic β-cell function.

1. Introduction

Diabetes mellitus is a growing public health concern in the United States, presently affecting 25.8 million or 8.3% of the American population [1]. This number is still increasing and is predicted to double by 2025 [2]. The medical costs associated with this disease, which include drug therapy and surgical treatment, are tremendous [1]. Diabetes is a complex metabolic disorder characterized by abnormalities in insulin secretion and action, which leads to hyperglycemia [3]. Type 1 diabetes (T1D) is a T-cell-mediated autoimmune disease leading to the destruction of pancreatic -cells, whereas type 2 diabetes (T2D) is due to a combination of peripheral insulin resistance and loss of functional -cell mass [47]. Therefore, in both T1D and T2D, inadequate -cell mass and -cell dysfunction leading to impaired insulin secretion are central to the deterioration of glycemic control [8]. Thus, the search for novel and cost-effective agents that can enhance -cell function and preserve -cell mass is important to provide effective treatment for diabetes.

Scutellariae baicalensis Georgi (SBG), a medicinal plant, grows in some Asian countries including Siberia, far East of Russia, Mongolia, China, and some other Eastern Asian countries [9]. The root of SBG has been used as an ingredient in traditional Chinese medicine formulations for thousands of years [10]. According to Chinese medicine, SBG has various beneficial effects on health. There have been 295 compounds isolated from SBG, more than 40 of which are flavonoids [11, 12]. Baicalein, baicalin, wogonin, and wogonoside are presumably the main bioactive components in SBG, which account for 5.41%, 10.11%, 1.3%, and 3.55%, respectively, of the dry material [13]. Recently, baicalein and its glucuronide baicalin have drawn wide attention due to their possible health effects. A recent study showed that oral administration of baicalin for 30 days reduced hyperglycemia-induced mitochondrial damage in -cells in diabetic rats [14]. Another study reported that long-term administration of baicalin reduced high-fat diet- (HFD-) induced body weight gain, circulating cholesterol and free fatty acid levels, lipid deposits in the liver, and systemic inflammation markers [15]. Studies on whether baicalein has an antidiabetic effect are scarce. Baicalein was reported to have beneficial effects in diabetes-associated health complications [1417], cancers [18, 19], cardiovascular disease [20], inflammation [21], bacterial infections [22, 23], and oxidative stress [2426], although some of the claimed benefits remain controversial and the mechanisms of these effects are unclear. In addition, it is unknown whether baicalein has an antidiabetic effect. Moreover, whether this compound exerts a beneficial effect on pancreatic -cells is unclear.

As aforementioned, loss of functional -cell mass and -cell dysfunction is central to the development of diabetes [8]. Thus, agents that can increase -cell mass and/or enhance -cell function can provide effective treatment for diabetes and thereby decrease the burden of morbidity from diabetes and related complications. In the present study, we evaluated the antidiabetic potential of baicalein in two mouse models and further determined its effects on pancreatic -cells. We found for the first time that baicalein improves hyperglycemia and glucose tolerance, promotes insulin secretion, and preserves islet mass by inhibiting apoptosis in middle-aged obese diabetic mice.

2. Materials and Methods

2.1. Materials

RPMI-1640 media (RPMI) were purchased from Sigma-Aldrich (St. Louis, MO); CMRL-1066 media (CMRL) were purchased from Mediatech (Holly Hill, FL); heat-inactivated fetal bovine serum (FBS) was obtained from HyClone (Logan, UT). Baicalein (98% pure) for in vitro studies was purchased from Sigma-Aldrich (St Louis, MO). Stock solutions of baicalein at 20 mM were dissolved in sterilized dimethyl sulfoxide (DMSO) and stored at −80°C before use. Baicalein (98% pure by HPLC) for in vivo studies was purchased from Xi’An Yile Bio-Tech Company, China; ultrasensitive rat insulin enzyme-linked immunosorbent assay (ELISA) kits were obtained from Mercodia (Winston-Salem, NC); the active form of the caspase-3 antibody was from BD Biosciences (San Jose, CA); the rabbit polyclonal anti-insulin antibody was from Abcam (Cambridge, MA); the ImmPRESS Anti-rabbit Ig (peroxidase) Polymer Detection kit, Vector NovaRED peroxidase substrate kit, and Vector SG peroxidase substrate kits were from Vector laboratories (Burlingame, CA); cell viability assay kits were from Promega (Madison, WI); and the BrdU ELISA kit for the cell proliferation assay was from Roche Applied Sciences (Indianapolis, IN). All other chemicals were from Sigma-Aldrich. Glucose was dissolved in sterile water and stored at −80°C.

2.2. Animals

Eight-month-old male C57BL/6 mice (National Cancer Institute, Frederick, MD) were individually housed in an animal room maintained on a 12 h light/dark cycle under constant temperature (22–25°C) with ad libitum access to food and water. After 1 wk of environment acclimation, the following two animal studies were performed. The animal study protocols were reviewed and approved by the Institutional Animal Care and Use Committee at Virginia Tech.

2.3. High-Fat Diet-Induced Obese Mice

For the first animal study, mice were divided into 3 groups () and fed either a standard diet (SD) with 10% of calories derived from fat, a high-fat diet (HF; Research Diets Inc., New Brunswick, NJ) with 58% of calories from fat, or HF supplemented with baicalein (0.5 g/kg diet) for 8 wks. Body weight (BW) and food intake were recorded weekly throughout the study. The fasting blood glucose levels in tail vein blood samples were measured using a glucometer (Roche) every 4 wk. After 7 wk of dietary baicalein supplementation, body composition was evaluated using an LF-90 instrument (Bruker Optics, Inc., Billerica MA). The LF-90 body composition instrument is based on time domain nuclear magnetic resonance (TD-NMR) technology which provides an in vivo measurement of lean tissue, body fat, and body fluid in live mice without anesthesia. At the end of 8 wk of dietary treatment, glucose tolerance and insulin tolerance tests were performed. For glucose tolerance tests, mice were fasted for 12 h and injected intraperitoneally (ip) with a single bolus of glucose (l g/kg BW). Glucose levels were measured at time points of 0, 15, 30, 60, and 120 min, and plasma insulin concentrations were measured at 0 and 30 min, after glucose administration. For the insulin tolerance test, mice were injected i.p. with insulin (0.75 units/kg BW), and blood glucose levels were measured at 0, 15, 30, 60, and 120 min after insulin administration. Area under the curve (AUC) was calculated using the trapezoidal rule. At the end of the study, blood samples were collected from overnight-fasted mice; plasma insulin concentration was measured using an ultrasensitive mouse/rat insulin ELISA kit; fasting plasma total cholesterol and triacylglycerols were measured in triplicate by enzymatic methods using a Pointer 180 Analyzer (Pointe Scientific, Canton, MI) as described [27].

2.4. Streptozotocin- (STZ-) Induced Diabetic Mice

For this study, mice were divided into 6 groups ( mice/group) with initial fasting blood glucose and body weights balanced among groups. Mice were then fed a SD diet, a HF diet (58 kcal% fat), or HF diet containing 0.25 g or 0.5 g baicalein/kg diet. After 4 wk of treatment, mice received ip injection of STZ dissolved in 0.1 M cold sterile sodium citrate buffer (pH 4.5) at 40 mg/kg daily for 3 consecutive days. Control mice received ip injection of saline. BW and food intake were measured weekly throughout the study. Fasting blood glucose levels were recorded every 2 wk before STZ injection. Following STZ injection, the levels of nonfasting blood glucose were measured weekly to assess the onset of hyperglycemia (nonfasting blood glucose >250 mg/dL) [27]. Plasma insulin concentration measurements and glucose tolerance and insulin tolerance tests were performed as stated above.

2.5. Immunohistochemistry

At the end of experiment, mice were euthanized, and the pancreata were dissected and fixed in 4% (vol/vol) formaldehyde buffer (pH 7.2). A series of tissue sections (5 μm thickness) were prepared by AML Laboratory (Baltimore, MD). For determining -cell mass, tissue sections mounted on glass slides were immunofluorescently stained with insulin antibody as we previously described [27]. The -cell area was measured using images acquired from insulin-stained pancreatic sections. The -cell mass was calculated by dividing the area of insulin-positive cells by the total area of pancreatic tissue and multiplying by the pancreas weight. The average was obtained from 10 mice in each group. The double labelling against the activated caspase-3 and insulin as a measure of -cell apoptosis was performed using an ImmPRESS detection system according to the manufacturer’s protocol. In brief, tissue sections were deparaffinized in xylene and rehydrated through a graded series of alcohol washes. Endogenous peroxidase activity was blocked by incubating in 3% H2O2 for 10 min. Antigen retrieval was carried out by boiling sections for 10 min in 0.01 M citrate buffer (pH 6.0), cooled at room temperature for 30 min, and then blocked with 2.5% normal horse serum in PBS for 20 min. Sections were then incubated with a rabbit-anti-mouse caspase-3 antibody detecting the activated form of caspase-3 (1 : 200 dilution) at room temperature for 1 h. Visualization was performed using a NovaRED peroxidase substrate kit. The slides were subsequently processed for double immunostaining for insulin using the same approach, and insulin was visualized using a SG peroxidase substrate kit. Five pancreatic sections from each mouse with 6 mice per group were costained with activated caspase-3 and insulin. Photographs of immune-stained pancreatic sections were captured using an Olympus phase contrast microscope.

2.6. Cell and Human Islet Culture

INS832/13 cells (kindly provided by Dr. Christopher Newgard at Duke University) were cultured in RPMI medium containing 11.1 mM glucose and supplemented with 10% FBS, 1 mM sodium pyruvate, 10 mM HEPES, 2 g/L sodium bicarbonate, 50 μM -mercaptoethanol, 100 U/mL penicillin, and 100 μg/mL streptomycin as previously described [27]. Medium was changed every 2-3 days until cells were approximately 70% confluent. Human islets were isolated from cadaver organ donors by the Islet Cell Resource Centers administered by the Southern California Resources Center & Southern California Islet Consortium at the National Medical Center (Duarte, CA). The islet purity was 90–99% and viability was 80–99%. Before the experiment, the islets were maintained in CMRL medium containing 10% FBS.

2.7. Insulin Secretion Assay

INS382/13 cells were cultured in 96-well plates in RPMI medium containing 11.1 mM glucose and 10% FBS at 37°C until the cells became 50%–60% confluent. The cultures were then switched to RPMI medium containing 3 mM glucose and 2% FBS for 12 h. For determining the effect of baicalein on glucose-stimulated insulin secretion (GSIS), cells and human islets were washed with Krebs-Ringer bicarbonate (KRB) buffer (129 mM NaCl, 4.8 mM KCl, 1.2 mM MgSO4, 1.2 mM KH2PO4, 2.5 mM CaCl2, 5 mM NaHCO3, 0.1% BSA, and 10 mM HEPES, pH 7.4) followed by incubation in KRB buffer containing 3 mM or 20 mM glucose in the presence or absence of 0.1, 1, 5, 10, or 20 μM baicalein at 37°C for 30 min. Insulin secreted in supernatants was measured by an ELISA kit. Human islets (100 islets/tube) were incubated in 3 or 20 mM glucose with or without various concentrations of baicalein in a 37°C water bath with gentle shaking for 30 min [28]. Insulin in the supernatants was measured by ELISA and normalized to protein content in the same sample. Our preliminary experiments showed that exposure of the cells to baicalein for 30 min had no effect on insulin or protein content.

2.8. Cell Viability Assay

INS382/13 cells or human islets were incubated with various concentrations of baicalein or vehicle in RPMI medium containing 5.5 mM glucose and 2% FBS at 37°C. 48 h later, the cultures were continued for an additional 4 h in the presence of 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS), a formazan compound, which was reduced by cells into a colored formazan product that was soluble in culture medium. Cell viability was assessed by the absorbance measurements at 490 nm with a plate reader. To determine whether baicalein has a protective effect on -cells exposed to chronic hyperlipidemia, INS382/13 cells or human islets (150 islets/well) were cultured in RPMI medium containing 0.5 mM palmitate or vehicle with or without various concentrations of baicalein for 4 d, with the medium replaced every other day. The cell viability was determined as stated above.

2.9. Cell Proliferation Assay

INS382/13 cells were incubated with various concentrations of baicalein or vehicle in RPMI medium containing 5.5 mM glucose and 2% FBS at 37°C. 24 h later, the cultures were continued for an additional 4 h in the presence of bromodeoxyuridine (BrdU), an analog of thymidine which incorporates into newly synthesized DNA, thereby labeling replicating cells. Cell proliferation was assessed by BrdU incorporation measurements with an ELISA cell proliferation assay kit as previously described [29].

2.10. Statistical Analyses

All data were analyzed with one-way ANOVA or Student’s -test using the SigmaPlot (Systat Software) program. Post hoc treatment comparisons were carried out with Tukey’s test. A was considered significant.

3. Results

3.1. Dietary Intake of Baicalein Had No Effects on Food Intake, Body Weight, Body Composition, and Plasma Lipid Profile in HF Diet-Induced Obese Mice

The HF diet decreased the accumulative average food intake, but baicalein supplementation for 8 consecutive wk did not alter the food consumption pattern compared with HF diet-fed mice (Figure 1(a)). Four wk of consuming HF diet significantly increased BW of mice. However, dietary intake of baicalein at 0.5 g/kg diet had no effect on HF diet-induced BW gain (Figure 1(b)). Baicalein treatment also had no effects on the weights of the heart, pancreas, spleen, liver, or kidney as compared to weights of HF mice (data not shown). Consistently, baicalein treatment did not alter body composition of obese mice as determined by measuring their relative percentage of fat (Figure 1(c)) and muscle mass (Figure 1(d)). Fasting blood levels of cholesterol (Figure 1(e)) and HDL-cholesterol (Figure 1(f)) were increased in HF diet-fed obese mice, but they were not significantly altered by dietary intake of baicalein. Fasting plasma triglyceride concentrations (Figure 1(g)) were not significantly altered by HF feeding or baicalein treatment.

3.2. Dietary Intake of Baicalein Improved Fasting Blood Glucose and Glucose Tolerance without Altering Peripheral Insulin Sensitivity in HF Diet-Induced Obese Mice

After 4 wk of HF diet consumption, mice displayed significantly elevated fasting blood glucose concentrations compared with animals that consumed the SD diet. Baicalein supplementation at this point did not affect the HF diet-induced rise in blood glucose. However, after 8 wks of baicalein supplementation, fasting blood glucose levels were significantly lower (30% reduction) than those in HF-fed mice (Figure 2(a)). Insulin resistance is important to the etiology of T2D and usually occurs in obesity. To determine if dietary intake of baicalein improves insulin sensitivity in obese mice, we performed an intraperitoneal insulin tolerance test. As expected, HF diet treatment impaired peripheral insulin sensitivity. However, there were little differences in plasma glucose levels (Figure 2(b)) and the AUC (Figure 2(c)) postinsulin injection between HF mice and mice given the HF diet supplemented with baicalein. These results suggest that the improvement in glucose tolerance in baicalein-treated mice is likely not due to an improvement in insulin sensitivity. We next performed a glucose tolerance test to evaluate if the improved glycemic control in mice that consumed baicalein-supplemented diets is via protecting pancreatic -cell function. Data showed that baicalein improved glucose tolerance as demonstrated by significantly lower blood glucose levels at 30 and 60 min (Figure 2(d)) as well as reduced AUC (Figure 2(e)) following intraperitoneal glucose injection compared to HF-fed mice. These results suggest that baicalein may promote pancreatic -cell insulin secretory function in response to glucose challenge. We then measured plasma insulin levels after overnight fasting and during intraperitoneal injection of glucose. We observed that fasting plasma insulin levels in HF mice were almost threefold of those in mice that received the SD diet, suggesting that obese mice are insulin resistant (Figure 3(a)). Baicalein treatment had no effect on fasting plasma insulin levels (Figure 3(a)) but significantly increased blood insulin concentrations following glucose injection (Figure 3(b)) indicating that the improvement in glucose tolerance in baicalein-treated mice may be the result of greater insulin secretion from pancreatic -cells.

3.3. Dietary Intake of Baicalein Ameliorated Hyperglycemia and Improved Insulin Levels in Middle-Aged Obese Diabetic Mice

We further assessed whether baicalein can prevent or ameliorate diabetes via promoting pancreatic -cell function in a T2D mouse model that was generated through a combination of HF diet feeding and three consecutive injections of low-doses of STZ [30]. Regarding this, C57BL/6 mice (male, 8 months old) were fed the SD, a HF, or HF containing 0.25 g, 0.5 g, or 1.0 g/kg baicalein. Treatment with baicalein for 4 wk had no effect on body weight gain, fasting blood glucose levels, or food intake of mice fed the HF diet (data not shown), consistent with the observations from the animal study described above. After 4 wk of dietary treatment, STZ (40 mg/kg BW) was administrated (ip) for 3 consecutive days to induce mild to moderate diabetes mediated by a destruction of islet -cells in mice [31]. Our data showed that baicalein significantly ameliorated STZ-induced hyperglycemia in diabetic mice fed 0.25 and 0.5 g/kg baicalein, with 0.5 g/kg baicalein producing the maximal protective effect (Figure 4(a)). Consistently, dietary ingestion of 0.25 and 0.5 g/kg baicalein ameliorated the loss of BW secondary to the development of diabetes [32] (Figure 4(b)), whereas food intake was not affected in diabetic mice (data not shown). In addition, insulin tolerance was not altered by baicalein treatment (data not shown), further confirming that this compound has no effect on insulin sensitivity. To determine if the improved glycemic control in mice that were fed the baicalein-supplemented diets is the result of improved islet function, we measured insulin levels in the plasma of control and baicalein-fed mice. As shown in Figure 4(c), plasma insulin levels in mice fed diets containing 0.25 and 0.5 g/kg baicalein were significantly greater as compared to those in nontreated diabetic mice, suggesting that baicalein may ameliorate hyperglycemia primarily through preserving islet -cell function.

3.4. Dietary Intake of Baicalein Improved Islet -Cell Mass in Obese Diabetic Mice

Since STZ causes diabetes by destroying islet -cells [33], and the results from our first animal study showed that baicalein might improve -cell function, we then examined whether baicalein treatment preserved -cell mass in diabetic mice by using an immunohistochemical technique. We found that STZ administration severely decreased -cell mass and insulin content and disrupted the islet architecture (Figures 5(a) and 5(b)). However, dietary provision of baicalein significantly improved islet -cell mass and preserved its structure in diabetic mice (Figures 5(a) and 5(b)). Consistently, baicalein-treated diabetic mice displayed fewer apoptotic -cells than untreated mice (Figure 5(c)), as determined by double immunolabeling of the activated caspase-3, a key protease involved in the terminal steps of cell apoptosis.

3.5. Baicalein Promoted Viability of Clonal -Cells and Human Islets

Our animal study showed that baicalein preserves functional -cell mass. To investigate the mechanism underlying this protective action of baicalein, we assessed whether baicalein affects the viability of insulin-secreting cells and human islets. Our results showed that baicalein dose-dependently increased both INS382/13 cell (Figure 6(a)) and human islet (Figure 6(b)) viability, with 5–20 μM exerting a protective action. To further determine whether baicalein is a survival factor for -cells, we evaluated whether baicalein protects clonal -cells and islets exposed to chronic hyperlipidemia. Incubation of INS382/13 cells (Figure 6(c)) or human islets (Figure 6(d)) with palmitate (0.5 mM) for 4 d significantly reduced cell viability. Addition of baicalein negated palmitate-induced reductions in cell viability, with 10 μM baicalein, completely abolished this detrimental effect of palmitate on the cells, suggesting that this compound may be capable of protecting against hyperlipidemia-induced -cell toxicity. It was reported that several flavonoids such as genistein can stimulate -cell proliferation [27]. We considered the possibility that baicalein may promote -cell survival by stimulating -cell proliferation. However, our results showed that baicalein at 0.1 μM to 20 μM concentrations had no effect on -cell proliferation as determined by a BrdU incorporation assay (data not shown).

3.6. Baicalein Promoted GSIS in Insulin-Secreting Cells and Human Islets

In the animal study, we found that baicalein may promote -cell function and insulin secretion in response to glucose. To examine whether baicalein directly enhances GSIS in -cells, we first cultured INS832/13 cells in basal (3 mM) or high (20 mM) glucose in the presence or absence of baicalein for 30 min. As shown in Figure 7(a), high glucose significantly induced insulin secretion and baicalein further dose-dependently augmented GSIS, with a maximal increase observed at a 10 μM concentration (Figure 7(a)). We then tested whether baicalein has a similar effect on insulin secretion in pancreatic islets. As shown in Figure 7(b), baicalein had no effect on basal insulin secretion but significantly augmented GSIS in human islets, suggesting that these in vitro findings may have physiological relevance.

4. Discussion

Baicalein is a major active constituent in the medicinal herb Scutellariae baicalensis Georgi. Previous studies showed that it has potential beneficial effects on several chronic diseases. Recent studies showed that baicalin, the glucuronide form of baicalein, may exert beneficial effects on diabetes mellitus or diabetes-related complications [1416]. However, whether and how baicalein exerts an antidiabetic effect is unclear. In the present study, we tested the antidiabetic potential of this natural compound using two mouse models, and we found that dietary intake of baicalein can improve glucose tolerance in middle-aged obese mice induced to become obese by HF diet feeding and ameliorate hyperglycemia in STZ-induced diabetic mice by preserving -cell mass and protecting its function. While peripheral insulin resistance is common during obesity and aging in mice and humans, its progression to T2D is largely due to insulin secretory dysfunction and significant apoptosis of functional -cells [5, 3437], leading to an inability to compensate for insulin resistance. Indeed, those with T2D always manifest increased -cell apoptosis and reduced -cell mass [35, 36, 38]. In this context, it is tempting to speculate that baicalein may be a plant-derived novel antidiabetic compound by protecting -cell mass and function, given that promotion or preservation of -cell mass has been shown to be effective in preventing and treating diabetes [5, 34, 3942].

In our animal studies, we used near middle-aged mice, because T2D usually occurs at middle and older ages in humans. We observed that baicalein treatment for 8 wks improved fasting blood glucose levels in obese mice. However, the mechanism by which baicalein treatment ameliorates fasting hyperglycemia is unclear, given that neither fasting plasma insulin levels nor peripheral insulin sensitivity was significantly modulated. A growing body of evidence indicates that obesity causes hepatic insulin resistance, leading to impaired regulation of glycogenolysis and gluconeogenesis by insulin, thereby increasing hepatic glucose production and output [43, 44]. Previous studies found that some of the flavonoids can reduce hepatic glucose production by suppressing the expression and enzymatic activities of phosphoenolpyruvate carboxykinase and glucose-6-phosphatase [4548], two critical enzymes for gluconeogenesis in the liver. It is unknown whether flavonoid baicalein also has this effect, which is currently under investigation in this laboratory. In this study, we also found that baicalein treatment improved glucose tolerance in obese mice, which should primarily reflect a direct response of -cells to circulating glucose, since whole body insulin sensitivity was not altered by baicalein treatment. Indeed, mice given baicalein displayed greater circulating insulin levels following ip injection of glucose compared to controls, suggesting that baicalein treatment may directly improve insulin secretion from pancreatic islets in response to a glucose challenge. We further explored whether baicalein directly protects pancreatic -cell function by using a nongenetic mouse model of T2D, that was generated by employing a combination of feeding a HF diet and administering three mild doses (40 mg/kg) of STZ that does not cause diabetes in chow-fed mice, as demonstrated in our previous study [30]. This nongenetic diabetic mouse model manifests the metabolic characteristics of human T2D, including moderate levels of hyperglycemia, hyperlipidemia, insulin resistance, impaired insulin secretion, and reduced -cell mass. The use of low-doses of STZ also minimizes the variability of diet-induced diabetes development and thus provides better experimental controls for evaluating the antidiabetic effects of this compound. The results in the present study show that baicalein protected against STZ-induced -cell apoptosis, thereby leading to the improved -cell mass in obese diabetic mice, which could be primarily attributable to its antidiabetic action, given that baicalein treatment did not alter other metabolic parameters such as insulin resistance, BW, or food intake.

Consistent with the animal data, we demonstrated that baicalein promoted insulin-secreting cell and pancreatic islet viability and insulin secretory function in vitro. Our results showing that 5 μM baicalein can improve the viability of INS1 and human islet cells and stimulate insulin secretion might be of biological relevance, given that this dose of baicalein used in the present study may overlap with the physiologically achievable levels in the plasma following dietary intake. It was reported that baicalein can be absorbed from the stomach and the small intestine due to its high lipophilicity and low molecular weight [49, 50]. In fact, it was found that after oral administration of baicalein to rodents, the plasma concentrations of total baicalein peaked at 10 μM and can be maintained at a 1 μM concentration for 36 h [51, 52]. Collectively, these results obtained from both in vivo and in vitro experiments strongly suggest that baicalein may act directly on the pancreatic -cell to enhance its function, thereby exerting an antidiabetic effect.

However, the exact mechanism underlying such a cytoprotective effect of this compound on -cells is presently unknown. 12/15-Lipoxygenase (LO) is a member of the LO family that catalyzes conversion of arachidonic acid to 12-hydroperoxyeicosatetraenoic acid, which is subsequently reduced to 12-hydroxyeicosatetraenoic acid, an inflammatory mediator [53]. 12/15-LO is expressed in both rodent and human islets and its expression and activity are upregulated in HF diet-induced obese mice [54]. Recent studies have shown that 12-LO knockout mice are resistant to islet -cell damage induced by HF feeding [54] or low-dose STZ administration [55], suggesting that this enzyme plays a crucial role in mediating metabolic stress-induced pancreatic -cell damage. Baicalein has been shown to be a potent inhibitor of 12/15-LO [56]. Therefore, it is intriguing to speculate that baicalein treatment may prevent islet -cells from HF feeding and STZ-induced damage, which is an ongoing investigation in this laboratory.

Our results show that baicalein could significantly stimulate insulin secretion in -cell lines and human islets. However, the mechanism is unclear. It is well characterized that glucose induces insulin secretion through glycolysis and mitochondrial oxidation in -cells. These events cause an increase in the intracellular ATP/ADP ratio, which sequentially leads to closure of KATP channels, depolarization of the cell membranes, Ca2+ influx, and ultimate exocytosis of insulin-containing granules [57]. Our in vitro study showed that baicalein treatment increases the viability of clonal -cells and human islets. Increased cell viability could produce more nicotinamide adenine dinucleotide (NADH) and nicotinamide adenine dinucleotide phosphate (NADPH), leading to enhanced mitochondrial function to increase ATP production, which may in turn enhance insulin secretion in -cells. Therefore, the effect of baicalein on insulin secretion may be mediated through improving mitochondrial metabolism, thereby increasing ATP generation in -cells [58]. There is also the possibility that baicalein stimulates insulin secretion through a cAMP-mediated mechanism. Cyclic AMP signaling plays an important role in -cell function including insulin secretion [59]. It was reported that genistein, a flavonoid from soybean, acutely stimulated insulin secretion in pancreatic -cells via a cAMP-dependent protein kinase pathway [28]. Baicalein was shown to activate the cAMP/PKA cascade in intestinal epithelial cells [60]. However, it is unknown whether baicalein can activate the cAMP/PKA pathway in -cells, leading to insulin secretion.

In summary, this is the first report to our knowledge that dietary supplementation of baicalein significantly ameliorated hyperglycemia and increased blood insulin levels, concomitant with improved functional islet mass, in obese diabetic mice. In addition, baicalein directly improved -cell and human islet viability and insulin secretion, suggesting that this natural compound may have a novel antidiabetic action. Future study should be directed at elucidating the molecular mechanism by which baicalein stimulates insulin secretion and promotes -cell survival.

Conflict of Interests

All authors declare that there is no conflict of interests regarding the publication of this paper.


The work was supported by Grants from National Center for Complementary and Alternative Medicine of National Institutes of Health (1R01AT007077, 1R01AT007566-01A1), the American Diabetes Association (7-11-BS-84 to D. Liu), and Diabetes Research and Action Education Foundation. Open access publication of this article is supported by Virginia Tech’s Open Access Subvention Fund. The contents of this paper are solely the responsibility of the authors and do not necessarily represent the official views of the funding agencies.


  1. ADA, “Total Prevalence of Diabetes & Pre-diabetes,” 2012. View at: Google Scholar
  2. H. King, R. E. Aubert, and W. H. Herman, “Global burden of diabetes, 1995–2025: prevalence, numerical estimates, and projections,” Diabetes Care, vol. 21, no. 9, pp. 1414–1431, 1998. View at: Publisher Site | Google Scholar
  3. S. Golbidi, S. A. Ebadi, and I. Laher, “Antioxidants in the treatment of diabetes,” Current Diabetes Reviews, vol. 7, no. 2, pp. 106–125, 2011. View at: Publisher Site | Google Scholar
  4. M. Knip and H. Siljander, “Autoimmune mechanisms in type 1 diabetes,” Autoimmunity Reviews, vol. 7, no. 7, pp. 550–557, 2008. View at: Publisher Site | Google Scholar
  5. D. A. Stoffers, “The development of beta-cell mass: recent progress and potential role of GLP-1,” Hormone and Metabolic Research, vol. 36, no. 11-12, pp. 811–821, 2004. View at: Publisher Site | Google Scholar
  6. A. M. Hennige, D. J. Burks, U. Ozcan et al., “Upregulation of insulin receptor substrate-2 in pancreatic β cells prevents diabetes,” The Journal of Clinical Investigation, vol. 112, no. 10, pp. 1521–1532, 2003. View at: Publisher Site | Google Scholar
  7. A. J. Scheen, “Diabetes mellitus in the elderly: insulin resistance and/or impaired insulin secretion?” Diabetes and Metabolism, vol. 31, no. 2, pp. S27–S34, 2005. View at: Google Scholar
  8. M. Stumvoll, B. J. Goldstein, and T. W. Van Haeften, “Type 2 diabetes: principles of pathogenesis and therapy,” The Lancet, vol. 365, no. 9467, pp. 1333–1346, 2005. View at: Publisher Site | Google Scholar
  9. M. Bruno, F. Piozzi, and S. Rosselli, “Natural and hemisynthetic neoclerodane diterpenoids from Scutellaria and their antifeedant activity,” Natural Product Reports, vol. 19, no. 3, pp. 357–378, 2002. View at: Publisher Site | Google Scholar
  10. Z. Hu, X. Yang, P. C. L. Ho et al., “Herb-drug interactions: a literature review,” Drugs, vol. 65, no. 9, pp. 1239–1282, 2005. View at: Publisher Site | Google Scholar
  11. X. Shang, X. He, M. Li et al., “The genus Scutellaria an ethnopharmacological and phytochemical review,” Journal of Ethnopharmacology, vol. 128, no. 2, pp. 279–313, 2010. View at: Publisher Site | Google Scholar
  12. K. Ishimaru, K. Nishikawa, T. Omoto, I. Asai, K. Yoshihira, and K. Shimomura, “Two flavone 2′-glucosides from Scutellaria baicalensis,” Phytochemistry, vol. 40, no. 1, pp. 279–281, 1995. View at: Publisher Site | Google Scholar
  13. M. Li-Weber, “New therapeutic aspects of flavones: the anticancer properties of Scutellaria and its main active constituents Wogonin, Baicalein and Baicalin,” Cancer Treatment Reviews, vol. 35, no. 1, pp. 57–68, 2009. View at: Publisher Site | Google Scholar
  14. V. Y. Waisundara, A. Hsu, B. K. Tan, and D. Huang, “Baicalin reduces mitochondrial damage in streptozotocin-induced diabetic Wistar rats,” Diabetes/Metabolism Research and Reviews, vol. 25, no. 7, pp. 671–677, 2009. View at: Publisher Site | Google Scholar
  15. H. X. Guo, D. H. Liu, Y. Ma et al., “Long-term baicalin administration ameliorates metabolic disorders and hepatic steatosis in rats given a high-fat diet,” Acta Pharmacologica Sinica, vol. 30, no. 11, pp. 1505–1512, 2009. View at: Publisher Site | Google Scholar
  16. P. Pu, X. Wang, M. Salim et al., “Baicalein, a natural product, selectively activating AMPKα2 and ameliorates metabolic disorder in diet-induced mice,” Molecular and Cellular Endocrinology, vol. 362, no. 1-2, pp. 128–138, 2012. View at: Publisher Site | Google Scholar
  17. M. A. Yorek, “Treatment of diabetic neuropathy with baicalein: intervention at multiple sites,” Experimental Neurology, vol. 232, no. 2, pp. 105–109, 2011. View at: Publisher Site | Google Scholar
  18. M. Himeji, T. Ohtsuki, H. Fukazawa et al., “Difference of growth-inhibitory effect of Scutellaria baicalensis-producing flavonoid wogonin among human cancer cells and normal diploid cell,” Cancer Letters, vol. 245, no. 1-2, pp. 269–274, 2007. View at: Publisher Site | Google Scholar
  19. S. Ikemoto, K. Sugimura, N. Yoshida et al., “Antitumor effects of Scutellariae radix and its components baicalein, baicalin, and wogonin on bladder cancer cell lines,” Urology, vol. 55, no. 6, pp. 951–955, 2000. View at: Publisher Site | Google Scholar
  20. Y. Huang, S. Tsang, X. Yao, and Z. Chen, “Biological properties of baicalein in cardiovascular system,” Current Drug Targets: Cardiovascular and Haematological Disorders, vol. 5, no. 2, pp. 177–184, 2005. View at: Publisher Site | Google Scholar
  21. L. Yang, H. Sun, L. Wu et al., “Baicalein reduces inflammatory process in a rodent model of diabetic retinopathy,” Investigative Ophthalmology and Visual Science, vol. 50, no. 5, pp. 2319–2327, 2009. View at: Publisher Site | Google Scholar
  22. D. L. Evers, C. Chao, X. Wang, Z. Zhang, S. Huong, and E. Huang, “Human cytomegalovirus-inhibitory flavonoids: studies on antiviral activity and mechanism of action,” Antiviral Research, vol. 68, no. 3, pp. 124–134, 2005. View at: Publisher Site | Google Scholar
  23. Z. Błach-Olszewska, B. Jatczak, A. Rak et al., “Production of cytokines and stimulation of resistance to viral infection in human leukocytes by Scutellaria baicalensis flavones,” Journal of Interferon and Cytokine Research, vol. 28, no. 9, pp. 571–581, 2008. View at: Publisher Site | Google Scholar
  24. X. Yang, W. He, W. Lu, and F. Zeng, “Effects of scutellarin on liver function after brain ischemia/reperfusion in rats,” Acta Pharmacologica Sinica, vol. 24, no. 11, pp. 1118–1174, 2003. View at: Google Scholar
  25. N. Lu, Y. Zhang, and Z. Gao, “Nitrite-glucose-glucose oxidase system directly induces rat heart homogenate oxidation and tyrosine nitration: effects of some flavonoids,” Toxicology in Vitro, vol. 23, no. 4, pp. 627–633, 2009. View at: Publisher Site | Google Scholar
  26. Y. Zhao, H. Li, Z. Gao, Y. Gong, and H. Xu, “Effects of flavonoids extracted from Scutellaria baicalensis Georgi on hemin-nitrite-H2O2 induced liver injury,” European Journal of Pharmacology, vol. 536, no. 1-2, pp. 192–199, 2006. View at: Publisher Site | Google Scholar
  27. Z. Fu, W. Zhang, W. Zhen et al., “Genistein induces pancreatic β-cell proliferation through activation of multiple signaling pathways and prevents insulin-deficient diabetes in mice,” Endocrinology, vol. 151, no. 7, pp. 3026–3037, 2010. View at: Publisher Site | Google Scholar
  28. D. Liu, W. Zhen, Z. Yang, J. D. Carter, H. Si, and K. A. Reynolds, “Genistein acutely stimulates insulin secretion in pancreatic β-cells through a cAMP-dependent protein kinase pathway,” Diabetes, vol. 55, no. 4, pp. 1043–1050, 2006. View at: Publisher Site | Google Scholar
  29. S. J. Brand, S. Tagerud, P. Lambert et al., “Pharmacological treatment of chronic diabetes by stimulating pancreatic β-cell regeneration with systemic co-administration of EGF and gastrin,” Pharmacology and Toxicology, vol. 91, no. 6, pp. 414–420, 2002. View at: Publisher Site | Google Scholar
  30. E. R. Gilbert, Z. Fu, and D. Liu, “Development of a nongenetic mouse model of type 2 diabetes,” Experimental Diabetes Research, vol. 2011, Article ID 416254, 12 pages, 2011. View at: Publisher Site | Google Scholar
  31. Z. Yang, M. Chen, L. B. Fialkow, J. D. Ellett, R. Wu, and J. L. Nadler, “The novel anti-inflammatory compound, lisofylline, prevents diabetes in multiple low-dose streptozotocin-treated mice.,” Pancreas, vol. 26, no. 4, pp. e99–e104, 2003. View at: Publisher Site | Google Scholar
  32. E. Larger, “Weight gain and insulin treatment,” Diabetes and Metabolism, vol. 31, no. 4, part 2, pp. 4S51–4S56, 2005. View at: Google Scholar
  33. W. J. Schnedl, S. Ferber, J. H. Johnson, and C. B. Newgard, “STZ transport and cytotoxicity: specific enhancement in GLUT2-expressing cells,” Diabetes, vol. 43, no. 11, pp. 1326–1333, 1994. View at: Publisher Site | Google Scholar
  34. C. Tourrel, D. Bailbe, M. Lacorne, M. Meile, M. Kergoat, and B. Portha, “Persistent improvement of type 2 diabetes in the Goto-Kakizaki rat model by expansion of the β-cell mass during the prediabetic period with glucagon-like peptide-1 or exendin-4,” Diabetes, vol. 51, no. 5, pp. 1443–1452, 2002. View at: Google Scholar
  35. H. Sakuraba, H. Mizukami, N. Yagihashi, R. Wada, C. Hanyu, and S. Yagihashi, “Reduced beta-cell mass and expression of oxidative stress-related DNA damage in the islet of Japanese Type II diabetic patients,” Diabetologia, vol. 45, no. 1, pp. 85–96, 2002. View at: Publisher Site | Google Scholar
  36. P. Marchetti, S. Del Guerra, L. Marselli et al., “Pancreatic islets from type 2 diabetic patients have functional defects and increased apoptosis that are ameliorated by metformin,” Journal of Clinical Endocrinology and Metabolism, vol. 89, no. 11, pp. 5535–5541, 2004. View at: Publisher Site | Google Scholar
  37. I. Cozar-Castellano, N. Fiaschi-Taesch, T. A. Bigatel et al., “Molecular control of cell cycle progression in the pancreatic β-cell,” Endocrine Reviews, vol. 27, no. 4, pp. 356–370, 2006. View at: Publisher Site | Google Scholar
  38. A. E. Butler, J. Janson, S. Bonner-Weir, R. Ritzel, R. A. Rizza, and P. C. Butler, “β-cell deficit and increased β-cell apoptosis in humans with type 2 diabetes,” Diabetes, vol. 52, no. 1, pp. 102–110, 2003. View at: Publisher Site | Google Scholar
  39. S. Sreenan, A. J. Pick, M. Levisetti, A. C. Baldwin, W. Pugh, and K. S. Polonsky, “Increased β-cell proliferation and reduced mass before diabetes onset in the nonobese diabetic mouse,” Diabetes, vol. 48, no. 5, pp. 989–996, 1999. View at: Publisher Site | Google Scholar
  40. W. L. Suarez-Pinzon, Y. Yan, R. Power, S. J. Brand, and A. Rabinovitch, “Combination therapy with epidermal growth factor and gastrin increases β-cell mass and reverses hyperglycemia in diabetic NOD mice,” Diabetes, vol. 54, no. 9, pp. 2596–2601, 2005. View at: Publisher Site | Google Scholar
  41. Q. Wang and P. Brubaker, “Glucagon-like peptide-1 treatment delays the onset of diabetes in 8 week-old db/db mice,” Diabetologia, vol. 45, no. 9, pp. 1263–1273, 2002. View at: Publisher Site | Google Scholar
  42. B. Rolin, M. O. Larsen, C. F. Gotfredsen et al., “The long-acting GLP-1 derivative NN2211 ameliorates glycemia and increases β-cell mass in diabetic mice,” The American Journal of Physiology: Endocrinology and Metabolism, vol. 283, no. 4, pp. E745–E752, 2002. View at: Google Scholar
  43. R. Basu, V. Chandramouli, B. Dicke, B. Landau, and R. Rizza, “Obesity and type 2 diabetes impair insulin-induced suppression of glycogenolysis as well as gluconeogenesis,” Diabetes, vol. 54, no. 7, pp. 1942–1948, 2005. View at: Publisher Site | Google Scholar
  44. R. A. Rizza, “Pathogenesis of fasting and postprandial hyperglycemia in type 2 diabetes: implications for therapy,” Diabetes, vol. 59, no. 11, pp. 2697–2707, 2010. View at: Publisher Site | Google Scholar
  45. M. E. Waltner-Law, X. L. Wang, B. K. Law, R. K. Hall, M. Nawano, and D. K. Granner, “Epigallocatechin gallate, a constituent of green tea, represses hepatic glucose production,” Journal of Biological Chemistry, vol. 277, no. 38, pp. 34933–34940, 2002. View at: Publisher Site | Google Scholar
  46. Q. F. Collins, H. Liu, J. Pi, Z. Liu, M. J. Quon, and W. Cao, “Epigallocatechin-3-gallate (EGCG), a green tea polyphenol, suppresses hepatic gluconeogenesis through 5′-AMP-activated protein kinase,” The Journal of Biological Chemistry, vol. 282, no. 41, pp. 30143–30149, 2007. View at: Publisher Site | Google Scholar
  47. M. S. Choi, U. J. Jung, J. Yeo, M. J. Kim, and M. K. Lee, “Genistein and daidzein prevent diabetes onset by elevating insulin level and altering hepatic gluconeogenic and lipogenic enzyme activities in non-obese diabetic (NOD) mice,” Diabetes/Metabolism Research and Reviews, vol. 24, no. 1, pp. 74–81, 2008. View at: Publisher Site | Google Scholar
  48. S. Ae Park, M. Choi, S. Cho et al., “Genistein and daidzein modulate hepatic glucose and lipid regulating enzyme activities in C57BL/KsJ-db/db mice,” Life Sciences, vol. 79, no. 12, pp. 1207–1213, 2006. View at: Publisher Site | Google Scholar
  49. L. Zhang, G. Lin, B. Kovács, M. Jani, P. Krajcsi, and Z. Zuo, “Mechanistic study on the intestinal absorption and disposition of baicalein,” European Journal of Pharmaceutical Sciences, vol. 31, no. 3-4, pp. 221–231, 2007. View at: Publisher Site | Google Scholar
  50. L. Taiming and J. Xuehua, “Investigation of the absorption mechanisms of baicalin and baicalein in rats,” Journal of Pharmaceutical Sciences, vol. 95, no. 6, pp. 1326–1333, 2006. View at: Publisher Site | Google Scholar
  51. J. Xing, X. Chen, and D. Zhong, “Absorption and enterohepatic circulation of baicalin in rats,” Life Sciences, vol. 78, no. 2, pp. 140–146, 2005. View at: Publisher Site | Google Scholar
  52. J. Xing, X. Chen, Y. Sun, Y. Luan, and D. Zhong, “Interaction of baicalin and baicalein with antibiotics in the gastrointestinal tract,” Journal of Pharmacy and Pharmacology, vol. 57, no. 6, pp. 743–750, 2005. View at: Publisher Site | Google Scholar
  53. X. Han, S. Chen, Y. Sun, J. L. Nadler, and D. Bleich, “Induction of cyclooxygenase-2 gene in pancreatic β-cells by 12-lipoxygenase pathway product 12-hydroxyeicosatetraenoic acid,” Molecular Endocrinology, vol. 16, no. 9, pp. 2145–2154, 2002. View at: Publisher Site | Google Scholar
  54. C. S. Nunemaker, M. Chen, H. Pei et al., “12-Lipoxygenase-knockout mice are resistant to inflammatory effects of obesity induced by Western diet,” American Journal of Physiology-Endocrinology and Metabolism, vol. 295, no. 5, pp. E1065–E1075, 2008. View at: Publisher Site | Google Scholar
  55. D. Bleich, S. Chen, B. Zipser, D. Sun, C. D. Funk, and J. L. Nadler, “Resistance to type 1 diabetes induction in 12-lipoxygenase knockout mice,” Journal of Clinical Investigation, vol. 103, no. 10, pp. 1431–1436, 1999. View at: Publisher Site | Google Scholar
  56. J. D. Deschamps, V. A. Kenyon, and T. R. Holman, “Baicalein is a potent in vitro inhibitor against both reticulocyte 15-human and platelet 12-human lipoxygenases,” Bioorganic and Medicinal Chemistry, vol. 14, no. 12, pp. 4295–4301, 2006. View at: Publisher Site | Google Scholar
  57. S. G. Straub and G. W. G. Sharp, “Glucose-stimulated signaling pathways in biphasic insulin secretion,” Diabetes/Metabolism Research and Reviews, vol. 18, no. 6, pp. 451–463, 2002. View at: Publisher Site | Google Scholar
  58. Y. Zhang and D. Liu, “Flavonol kaempferol improves chronic hyperglycemia-impaired pancreatic beta-cell viability and insulin secretory function,” European Journal of Pharmacology, vol. 670, no. 1, pp. 325–332, 2011. View at: Publisher Site | Google Scholar
  59. N. Dachicourt, P. Serradas, M.-H. Giroix, M.-N. Gangnerau, and B. Portha, “Decreased glucose-induced cAMP and insulin release in islets of diabetic rats: reversal by IBMX, glucagon, GIP,” American Journal of Physiology, vol. 271, no. 4, part 1, pp. E725–E732, 1996. View at: Google Scholar
  60. G. G. Yue, T. W. Yip, Y. Huang, and W. Ko, “Cellular mechanism for potentiation of Ca2+-mediated Cl− secretion by the flavonoid baicalein in intestinal epithelia,” Journal of Biological Chemistry, vol. 279, no. 38, pp. 39310–39316, 2004. View at: Publisher Site | Google Scholar

Copyright © 2014 Yu Fu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.